Colon Cancer: Gene >> BMP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378827
Start	6770352:6770352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226C>A
AA Mutation	p.Pro76Thr(p.P76T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378827
Start	6778407:6778407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776834114
CDS Mutation	c.509G>A
AA Mutation	p.Arg170Gln(p.R170Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378827
Start	6778727:6778727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829C>A
AA Mutation	p.His277Asn(p.H277N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378827
Start	6770418:6770418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756645581
CDS Mutation	c.292C>T
AA Mutation	p.Arg98Trp(p.R98W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378827
Start	6778562:6778562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140884062
CDS Mutation	c.664G>A
AA Mutation	p.Ala222Thr(p.A222T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378827
Start	6770377:6770377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251G>A
AA Mutation	p.Arg84His(p.R84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378827
Start	6770250:6770250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.124T>G
AA Mutation	p.Ser42Ala(p.S42A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000378827
Start	6778877:6778877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190569855
CDS Mutation	c.979G>A
AA Mutation	p.Gly327Arg(p.G327R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378827
Start	6770156:6770156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.30G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378827
Start	6778576:6778576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770008690
CDS Mutation	c.678C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378827
Start	6778314:6778315(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.420dupC
AA Mutation	p.Thr141HisfsTer25(p.T141Hfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BMP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378827
Start	6778407:6778407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776834114
CDS Mutation	c.509G>A
AA Mutation	p.Arg170Gln(p.R170Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378827
Start	6779047:6779047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149G>T
AA Mutation	p.Lys383Asn(p.K383N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378827
Start	6778786:6778786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888T>C
Mutation Classification	Silent
Feature Type	Transcript